Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Cuisinart Recall Impacts 8 Million Food Processors, Due to Risk of Broken Blade Pieces December 14, 2016 Russell Maas Add Your CommentsMore than 8 million Cuisinart food processors have been recalled, following dozens of reports involving problems where pieces of the metal blades broke off into the food, resulting in at least 30 consumer complaints involving mouth lacerations and tooth injuries.ย The Cuisinart food processor recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on December 13, following at least 69 consumer complaints that suggest the riveted metal blades may crack and break off into the food being processed. To date, injuries caused by the recalled food processors appear to involve cuts to the interior of the mouth and tooth damage caused by the metal blade pieces.Federal safety officials are recalling the Cuisinart food processors due to the severity and variety of hazards posed by the breaking blades. Cuisinart reports that the riveted blades may become worn over time and can crack into small metal pieces, which can then be processed into the food.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONIn addition to a risk of mouth and tooth injuries, the Cuisinart food processor blade pieces may cause choking or internal organ laceration hazards if the fragments are fully consumed. The CPSC recommends customers stop using the recalled food processors immediately and check the blades to determine whether any food previously processed and stored away could have broken riveted blade fragments in it.The recall includes Cuisinart food processors equipped with riveted blades that are silver colored stainless steel with a beige plastic center hub. The recalled processors have model numbers that begin with CFP-9, CFP-11, DFP-7, DFP-11, DFP-14, DLC-5, DLC-7, DLC-8, DLC-10, DLC-XP, DLC-2007, DLC-2009, DLC-2011, DLC-2014, DLC-3011, DLC-3014, EV-7, EV-10, EV-11, EV-14, KFP-7 or MP-14. The brand name Cuisinart is printed on both the front base and bottom of the food processors and according to the CPSC, only the food processors with four rivets in the blades are included in the recall.The CPSC indicates that roughly 8 million units were sold in the United States, with an additional 300,000 were distributed for sale in Canada.The Cuisinart food processors were manufactured in China under Conair Corporation of Stamford, Connecticut. They were distributed for sale at department, gourmet and specialty stores nationwide and through various online retailers from July 1996 through December 2015 for between $100 and $350.Customers are being asked to stop using the devices immediately and to contact Cuisinart toll-free at 877-339-2534 or visit them online at www.cuisinart.com and navigate to the โProduct Recallsโ link at the bottom of the page for information on how to receive a free replacement blade. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Appliance Recall, Cuisinart, Cuisinart Food Processor, LacerationMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 0 Comments URLThis field is for validation purposes and should be left unchanged.Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes NoPost Comment I authorize the above comments be posted on this pageWeekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings.Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermΔ MORE TOP STORIES Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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